Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Tmf Classifier I

Fortrea
0-2 years
₹3.5–5.5 LPA
Bangalore, India
15 July 7, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Analytical Characterization, Dissolution Testing, Experimental Design, GMP/cGMP Compliance, HPLC, HPLC Analysis, Pre-formulation Studies, Regulatory Filing Support, Root Cause Analysis (RCA), Technology Transfer, UPLC

TMF Classifier I

Location: Bangalore
Department: Clinical
Employment Type: Full-Time

Experience: 6 months–1 year of experience in a clinical research environment with exposure to TMF/eTMF management, document classification, or clinical operations.
Salary Package: ₹3.5–5.5 LPA (Approx., based on current market standards; final compensation depends on candidate experience and skills.)


Role Overview

The TMF Classifier I is responsible for managing document classification within the electronic Trial Master File (eTMF), ensuring documents are audit-ready, compliant with regulatory requirements, and accurately maintained throughout the clinical trial lifecycle.


Key Responsibilities

TMF Management

  • Manage document classification under Smart Inbox and ARC Review (as applicable).

  • Perform document deletion and maintain accurate document records.

  • Manage Trial, Country, and Site artifacts within the electronic Trial Master File (eTMF).

  • Collaborate with study teams to ensure timely and accurate document management.

Quality & Compliance

  • Maintain TMF in an audit-ready state by ensuring document quality and completeness.

  • Perform visual quality checks to verify document clarity and readability.

  • Conduct Audit Ready Checks to ensure document accuracy and compliance.

  • Process and track essential study documents throughout all phases of clinical trials.

  • Ensure compliance with company SOPs, sponsor SOPs, Good Clinical Practice (GCP), and ICH guidelines.

Regulatory Support

  • Maintain knowledge of applicable regulatory requirements.

  • Identify and resolve operational issues related to TMF management.

  • Prepare TMFs for internal QA and sponsor audits.

  • Implement corrective actions based on audit findings.

  • Participate in internal and client audits as required.

Collaboration & Process Improvement

  • Collaborate with cross-functional teams to support study execution.

  • Attend internal and external study meetings when required.

  • Contribute to continuous process improvement initiatives to enhance quality and productivity.

  • Ensure high levels of client satisfaction across assigned studies.

  • Perform additional responsibilities as assigned.


Educational Qualification

  • Bachelor's Degree in Life Sciences, Pharmacy, Biotechnology, Business, or a related field.

  • Master's Degree in Life Sciences or Business is preferred.


Required Experience

  • 6 months–1 year of experience in a clinical research environment.

  • Experience working with electronic Trial Master Files (eTMF) or clinical documentation is preferred.


Technical Skills

  • Knowledge of Good Clinical Practice (GCP) and ICH Guidelines.

  • Understanding of Regulatory and Clinical Trial documentation requirements.

  • Experience with eTMF systems and clinical electronic systems is preferred.

  • Proficiency in Microsoft Office Suite and Adobe Acrobat.

  • Familiarity with document scanning and electronic document management systems.


Key Competencies

  • Strong attention to detail and document quality.

  • Excellent organizational and time management skills.

  • Strong communication and interpersonal abilities.

  • Ability to work collaboratively in cross-functional teams.

  • Analytical and problem-solving skills.

  • Commitment to regulatory compliance and audit readiness.

  • Ability to manage multiple priorities in a fast-paced clinical environment.


Travel Requirement

  • Minimal travel (less than 10%) for Sponsor Kick-Off Meetings, client meetings, and study-related activities as required.